The DOI matches its Crossref record; 5 of the 5 references it cites were found in a registry or an index.
Kisspeptin Acts Directly and Indirectly to Increase Gonadotropin-Releasing Hormone Neuron Activity and Its Effects Are Modulated by Estradiol
Open accessAbstract
GnRH neurons play a pivotal role in the central regulation of fertility. Kisspeptin greatly increases GnRH/LH release and GnRH neuron firing activity and may be involved in estradiol feedback, but the neurobiological mechanisms for these actions are unknown. G protein-coupled receptor 54, the receptor for kisspeptin, is expressed by GnRH neurons as well as other hypothalamic neurons, suggesting both direct and indirect effects are possible. To investigate this and determine whether kisspeptin activation of GnRH neurons is estradiol sensitive, we recorded the firing rate of GnRH neurons in brain slices from adult female mice that were ovariectomized (OVX) and either treated with estradiol (E) capsules (OVX+E) or left without further treatment. Kisspeptin increased GnRH neuronal activity in a dose-dependent manner in cells from both OVX and OVX+E mice, and estradiol significantly potentiated the response. To begin to distinguish direct from indirect actions of kisspeptin, fast synaptic transmission mediated by ionotropic γ-aminobutyric acid and glutamate receptors was pharmacologically blocked (blockade). Blockade reduced GnRH response to kisspeptin in OVX+E but not in OVX mice. Actions of kisspeptin were also assessed using whole-cell voltage- and current-clamp recording in slices from OVX animals. Kisspeptin application depolarized GnRH neurons in current-clamp and generated inward current in voltage-clamp recordings, even after blocking action potential-dependent neural communication, consistent with a direct effect. Blockers of potassium channels abolished the inward current. Together our data indicate that kisspeptin activates GnRH neurons via both direct and transsynaptic mechanisms and that transsynaptic mechanisms are either enabled and/or potentiated by estradiol.
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The GPR54 Gene as a Regulator of Puberty
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Hypogonadotropic hypogonadism due to loss of function of the KiSS1-derived peptide receptor GPR54
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Regulation of Kiss1 gene expression in the brain of the female mouse
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Cited by
Kisspeptin Signaling in the Brain
Oakley, A. E., Clifton, D. K., & Steiner, R. A. (2009) · Endocrine Reviews · doi:10.1210/er.2009-0005 · Cited by 842
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“duces a prolonged activation of GnRH neurons in the mouse (Han et al., 2005; Pielecka-Fortuna et al., 2008).”
BackgroundResultRoseweir, A. K., Kauffman, A. S., Smith, J. T., Guerriero, K. A., Morgan, K., Pielecka-Fortuna, J., Pineda, R., Gottsch, M. L., Tena-Sempere, M., Moenter, S. M., et al. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.5740-08.2009 · Cited by 379
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The neurobiology of preovulatory and estradiol-induced gonadotropin-releasing hormone surges
Christian, C. A., & Moenter, S. M. (2010) · Endocrine Reviews · doi:10.1210/er.2009-0023 · Cited by 300
Self-citationNeuroanatomy of the kisspeptin signaling system in mammals: comparative and developmental aspects
Lehman, M. N., Hileman, S. M., & Goodman, R. L. (2013) · Advances in Experimental Medicine and Biology · doi:10.1007/978-1-4614-6199-9_3 · Cited by 180
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Neuroendocrine Control of the Ovarian Cycle of the Rat
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Kisspeptin resets the hypothalamic GnRH clock in men
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Coming of age in the Kisspeptin Era: Sex differences, development, and puberty
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17β-Estradiol Regulation of T-Type Calcium Channels in Gonadotropin-Releasing Hormone Neurons
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Estrogenic Regulation of the GnRH Neuron
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Self-citationSmith, J. T. (2012) · Domestic Animal Endocrinology · doi:10.1016/j.domaniend.2011.11.003 · Cited by 55
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Self-citation
Metadata
- Authors
- Pielecka-Fortuna, J., Chu, Z., & Moenter, S. M.
- Venue
- Endocrinology
- Publisher
- The Endocrine Society
- Published
- 2007-12-27
- Volume
- 149
- Issue
- 4
- Pages
- 1979-1986
- ISSN
- 0013-7227 (ISSN-L)
- 1945-7170
- OpenAlex
- W2071540424
- Cited by
- 345
- References
- 5
- FWCI
- 17.52
- Type
- journal article
- Language
- en
- Open access
- bronze
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